Kabir Md Arafat, Murata Masaru, Shakya Mamata, Yamada Katsuhisa, Akazawa Toshiyuki
Division of Oral Regenerative Medicine, School of Dentistry, Health Sciences University of Hokkaido, 1757 Kanazawa, Hokkaido 061-0293, Japan.
Department of Orthopaedic Surgery, Faculty of Medicine and Graduate of Medicine, Hokkaido University, Kita 8 Jonishi 5-chome, Kita-ku, Sapporo, Hokkaido 060-0808, Japan.
Materials (Basel). 2021 Jan 5;14(1):223. doi: 10.3390/ma14010223.
The aim of this study was to evaluate the bio-absorption and bone regeneration of human tooth-derived dentin scaffold, entitled as perforated root-demineralized dentin matrix (PR-DDM), after in vivo implantation into the critical-size iliac defects. The dentin scaffolds were prepared from human vital, non-functional teeth. Thirty artificial macro-pores (Ø 1 mm) were added after removing the enamel portion. The modified teeth were supersonically demineralized in 0.34 N HNO for 30 min. The microstructure was observed by scanning electron microscope (SEM). The 3D micro-CT and histological analysis were carried out to evaluate the bio-absorption of PR-DDM at 2 and 4 months. A smooth dentin collagen surface with symmetrical macro-pores and tube-type dentinal tubules (Ø 1-2 µm) with micro-cracks were observed on the perforated region. A significant number of custom-made macro-pores disappeared, and the size of the macro-pores became significantly wider at 4 months compared with the 2 months ( < 0.05) evaluated by 3D micro-CT. Histological images revealed the presence of multinucleated giant cells attached to the scalloped border of the PR-DDM. The morphological changes due to bio-absorption by the cellular phagocytes were comparable to the 3D micro-CT and histological images at 2 and 4 months. Altogether, the results demonstrated that the PR-DDM block was gradually absorbed by multinucleated giant cells and regenerated bone. Human PR-DDM might serve as a unique scaffold for extraoral bone regeneration.
本研究的目的是评估一种名为穿孔牙根脱矿牙本质基质(PR-DDM)的人牙源性牙本质支架在体内植入临界大小的髂骨缺损后其生物吸收和骨再生情况。牙本质支架由人类活的、无功能的牙齿制备而成。去除牙釉质部分后添加30个人工大孔(直径1毫米)。将改良后的牙齿在0.34N硝酸中超声脱矿30分钟。通过扫描电子显微镜(SEM)观察微观结构。在2个月和4个月时进行三维显微CT和组织学分析,以评估PR-DDM的生物吸收情况。在穿孔区域观察到光滑的牙本质胶原表面,有对称的大孔以及带有微裂纹的管状牙本质小管(直径1-2微米)。通过三维显微CT评估发现,与2个月时相比,4个月时大量定制的大孔消失,且大孔尺寸明显变宽(P<0.05)。组织学图像显示有多核巨细胞附着在PR-DDM的扇贝状边缘。细胞吞噬作用引起的生物吸收导致的形态变化与2个月和4个月时的三维显微CT及组织学图像结果相当。总之,结果表明PR-DDM块被多核巨细胞逐渐吸收并再生出骨组织。人PR-DDM可能作为一种独特的支架用于口腔外骨再生。